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Monothérapie Bithérapie Trithérapie Autres Molécule

Dose

Début à j .. /durée

Désescalade thérapeutique : oui □ àj … Non □

Evolution

: ÆFavorable □ Critère clinique/paraclinique Défervescence thermique Nettoyage expectorations Bonne saturation disparition foyer Rx ↓ GB ↓CRP Autre Oui / non ÆDéfavorable □ Décès par :

Tableau I : Le Clinical Pulmonary Infection Score (CPIS) [76] Température ≥ 36,5 °C et ≤ 38,4 °C 0 point ≥ 38,5 °C et ≤ 38,9 °C 1 point ≤ 36 °C ou ≥ 39 °C 2 points Leucocytose ≥ 4 G/L et ≤ 11 G/L 0 point < 4 G/L ou > 11 G/L 1 point si formes immatures ≥ 0,5 G/L +1 point Aspirations trachéales

< 4 + de sécrétions 0 point

≥ 4 + de sécrétions 1 point

si sécrétions purulentes +1 point PaO2/FIO2

> 240 ou SDRA 0 point

≤ 240 sans SDRA 2 points

Radiographie thoracique

absence d'infiltrat 0 point

infiltrat diffus 1 point

infiltrat localisé 2 points

Culture semi-quantitative des sécrétions trachéales (0, 1, 2 ou 3 +)

bactérie pathogène ≤ 1+ 0 point bactérie pathogène > 1+ 1 point si même bactérie sur Gram +1 point

Tableau II : Antibiothérapie probabiliste initiale recommandée selon le délai de survenue de la PNAVM et l’existence de facteurs de risque de BMR (adapté de [7] en 2005).

PN à début précoce (< 5 jours), sans facteurs de risque De BMR*, quelle que soit la gravité

PN à début tardif (> 5 jours) ou avec facteurs de risque de BMR*, quelle que soit la gravité

Germes potentiellement En cause ATB à spectre étroit Germes potentiellement en cause ATB à large spectre Cocci Gram+ S. Pneumoniae SAMS BGN : H. influenzae BG sensible E. coli Klebsiella pneumoniae Enterobacter spp. Serratia marcescens C3G ou Ampicilline+inhibiteur des β lactamases ou Fluoro-quinolones1 ou Ertapénème Cocci Gram+ et BGN précédents+ BMR P. aeruginosa K.pneumoniae(BLSE)* Acinetobacter sp.(BLSE)* + SAMR Legionelle pneumophila** C3G anti- pseudomonas² ou

Carbapénème anti- pseudomonas3 ou ßlactamine+inhibiteur de ßlactamases4 + Fluoro-quinolones anti-pseudomonas5 ou Aminoglycosides6 + vancomycine ou linézolide BMR* : bactéries multi-résistantes ,

1 : préfrer lévofloxacine ou moxifloxacine à la ciprofloxacine, 2 : céftazidime, céfipime,

3 : imipénème, méropénème, 4 : pipéracilline tazobactam, 5 : ciprofloxacine, lévofloxacine,

6 : amikacine, gentamycine ou tobramycine,

* :si suspicion de souche BLSE (bétalactamases à spectre élargie),on choisi les carbapénèmes, * *: association doit comporter un macrolide ou une fluoro-quinolone

Résumé

Les pneumopathies nosocomiales acquises sous ventilation mécanique (PNAVM) sont des causes principales de mortalité des patients hospitalisés en réanimation.

Ce travail consiste en une analyse épidémiologique des PNAVM dans le but d’évaluer l’incidence, les facteurs de risque, l’écologie bactérienne locale, le profil des résistances des germes, la stratégie thérapeutique, le pronostic et d’en déduire des mesures préventives.

C’est une étude rétrospective d’une série de 109 cas, hospitalisés en service de réanimation polyvalente du CHU Mohamed VI de Marrakech durant la période 2003-2007 et qui ont présenté une PNAVM.

L’incidence a été de 4,24%. Le diagnostic des PNAVM se base sur des critères cliniques, biologiques, radiologiques et bactériologiques avec essentiellement le prélèvement bronchique distal protégé dans nôtre série.

Le facteur de risque majeur a été la durée de la ventilation artificielle avec une moyenne de 15 jours (±10.09).

Les BGN représentent 61.4% des germes isolés (pseudomonas aéruginosae 38,5% , acinétobacter baumanii 22.7% , entérobacter cloacae 11.3%). Les cocci Gram positif représentent 30.5%, dont le staphylocoque en chef de fil avec prédominance du staphylocoque sensible à la méthiciline (SAMS) : 24,7%, SARM / SAMS = 0.33 (SARM : staphylocoque aureus résistant à la méthiciline).

Le traitement antibiotique s’est basé surtout sur la bithérapie 57.8% versus 38.5% pour la trithérapie utilisant surtout l’imipenème et l’amikacine avec une antibiothérapie orientée pour 49% versus empirique pour 51% des patients.

La mortalité est estimée à 51.4% contre une évolution favorable pour48,6% des patients. Le pronostic des PNAVM est corrélé au terrain, aux soins prodigués, au type de germe, au type et à la durée de l’antibiothérapie.

Au terme de ce travail nous proposons des mesures préventives se basant surtout sur le respect des règles d’hygiène et la formation continue du personnel vis-à-vis de ces mesures.

Summary

Nosocomial pneumopathies acquired under mechanical ventilation (PNAVM) are main causes of mortality of the patients hospitalized in reanimation.

This study consists of an epidemiological analysis of the PNAVM with the aim of estimating the incidence, the risk factors, the local bacterial ecology, the profile of the resistances of germs, the strategy Therapeutics, the forecast and to deduce from precautionary measures.

It is a retrospective study of series of 109 cases, hospitalized in reanimation of Mohamed VI Teaching Hospital of Marrakech during the period 2003-2007 and presenting PNAVM with an incidence of 4,24% and.

The PAVM diagnosis is based on clinical, biological, radiological and bacteriological criteria and mainly in our series the protected bronchial distal sampling. The major risk factor was the duration of the artificial ventilation with average of 15 days ( ±10.09 ).

The BGN represents 61.4 % of germs isolated (pseudomonas aeruginosae 38,5 %, Acinetobacter baumanii 22.7 %, enterobacter cloacae 11.3 %). The cocci Gram positive represent 30.5 % ; Staphylococcus are in the lead with predominance of staphylococcus sensitive to the methicilin (SAMS): 24,7% SARM/ SAMS= 0.33.

The antibiotic treatment is mainly based on the bitherapy 57.8 % versus 38.5 % for the tritherapy using especially the imipeneme and the amikacine with an antibiotic treatment adapted for 49.1 % versus empirical for 42.5%. The mortality is estimated at 51.4 % in ours series against a favorable evolution for 48,6 % of the patients.

The prognosis of the PNAVM is correlated with the ground, the lavished care, the type and duration of antibiotic treatment.

Finally, we suggest precautionary measures based especially on the respect of hygienization and an in-service training of the staff towards these measures.

ﺺﺨﻠﻣ

ﻥﻋ ﺞﺘﺎﻨﻟﺍﻭ ﻰﻔﺸﺘﺴﻤﻟﺍ ﻲﻓ لﻭﻤﺤﻤﻟﺍ ﻱﻭﺌﺭﻟﺍ ﺏﺎﻬﺘﻟﻻﺍ ﺩﻌﻴ

ﺔﻴﺴﻴﺌﺭﻟﺍ ﺏﺎﺒﺴﻷﺍ ﻥﻤ ﺔﻴﻋﺎﻨﻁﺼﻹﺍ ﺔﻴﻭﻬﺘﻟﺍ

ﺓﺯﻜﺭﻤﻟﺍ ﺔﻴﺎﻨﻌﻟﺍ ﺡﺎﻨﺠﺒ ﻥﻴﻤﻴﻘﻤﻟﺍ ﻰﻀﺭﻤﻟﺍ ﺕﺎﻴﻓﻭﻟ

.

،ﺭﻁﺨﻟﺍ ﺭﺼﺎﻨﻋﻭ ﻉﻭﻗﻭﻟﺍ ﺔﺒﺴﻨ ﻡﻴﻴﻘﺘ لﺠﺃ ﻥﻤ ﺀﺍﺩﻟﺍ ﺍﺫﻬﻟ ﺎﻴﺌﺎﺒﻭ ﻼﻴﻠﺤﺘ ،ﺔﺴﺍﺭﺩﻟﺍ ﻩﺫﻫ ﻥﻤﻀﺘﺘ

ﺤﻤﻟﺍ ﺕﺎﻴﺭﻴﺘﻜﺒﻟﺍ ﺔﻴﻋﻭﻨ ﺩﻴﺩﺤﺘﻭ

ﻡﺘ ﻥﻤﻭ ،ﺽﺭﻤﻟﺍ ﺭﻴﺼﻤﻭ ﺔﻴﺠﻼﻌﻟﺍ ﺔﻴﺠﻴﺘﺍﺭﺘﺴﻹﺍ ﺍﺫﻜﻭ ﺎﻬﺘﻤﻭﺎﻘﻤ ﻁﻤﻨﻭ ﺔﻴﻠ

لﺌﺎﺴﻭﻟﺍ ﺝﺎﺘﻨﺘﺴﺍ

ﺔﻴﺌﺎﻗﻭﻟﺍ

.

ﻥﻤ ﺔﻨﻭﻜﻤ ﺔﻋﻭﻤﺠﻤ ﻥﻤ ﺔﻴﺩﺎﻌﻴﺘﺴﻹﺍ ﺔﺴﺍﺭﺩﻟﺍ ﻩﺫﻫ ﻥﻭﻜﺘﺘ

109

ﺔﻴﺎﻨﻌﻟﺍ ﺡﺎﻨﺠﺒ ﻡﻫﺅﺎﻔﺸﺘﺴﺍ ﻡﺘ ﺽﻴﺭﻤ

ﻥﻴﺒ ﺎﻤ ﺵﻜﺍﺭﻤﺒ ﺱﺩﺎﺴﻟﺍ ﺩﻤﺤﻤ ﻲﻌﻤﺎﺠﻟﺍ ﻰﻔﺸﺘﺴﻤﻟﺎﺒ ﺓﺯﻜﺭﻤﻟﺍ

2003

2007

ﺍﻭﻨﺎﻋ ﻥﻴﺫﻟﺍﻭ

ﻱﻭﺌﺭ ﺏﺎﻬﺘﻟﺍ ﻥﻤ

ﺔﺒﺴﻨﺒ ﺔﻴﻋﺎﻨﻁﺼﻹﺍ ﺔﻴﻭﻬﺘﻟﺍ ﻥﻋ ﺞﺘﺎﻨ

4.24

%

.

ﺯﻴﻜﺭﺘﻟﺍ ﻊﻤ ﺔﻴﺠﻭﻟﻭﻴﺭﻴﺘﻜﺒﻭ ﺔﻴﻋﺎﻌﺸ ،ﺔﻴﺠﻭﻟﻭﻴﺒ ،ﺔﻴﺭﻴﺭﺴ ﺭﻴﻴﺎﻌﻤ ﻰﻠﻋ ﺽﺭﻤﻟﺍ ﺍﺫﻫ ﺹﻴﺨﺸﺘ ﺩﻤﺘﻌﻴ

،ﺔﻴﺌﺍﻭﻬﻟﺍ ﺏﻌﺸﻟﺍ ﻥﻤ ﺓﺩﻴﻌﺒ ﺔﻴﻤﺤﻤ ﺕﺎﻨﻴﻋ ﺫﺨﺃ ﻰﻠﻋ ﺱﺎﺴﻷﺎﺒ ﺎﻨﺘﺴﺍﺭﺩ ﻲﻓ

ﻤﺒ ﻲﺴﻴﺌﺭﻟﺍ ﺭﻁﺨﻟﺍ لﻤﺎﻋ ﺔﻴﻋﺎﻨﻁﺼﻻﺍ ﺔﻴﻭﻬﺘﻟﺍ ﺓﺩﻤ ﺩﻌﺘ

ﻁﺴﻭﺘ

15

ﺎﻤﻭﻴ

)

10،09

(

ﻡﺍﺭﻐﻟﺍ ﺔﻴﺒﻠﺴﻟﺍ ﺕﺎﻴﺼﻌﻟﺍ لﺜﻤﺘ

61,4%

ﺔﻟﻭﺯﻌﻤﻟﺍ ﻡﻴﺜﺍﺭﺠﻟﺍ ﻉﻭﻤﺠﻤ ﻥﻤ

)

ﺔﺒﺴﻨﺒ ﺱﺎﻨﻭﻤﻭ ﺩﻭﺴﺒﻟﺍ

38,5%

ﺔﺒﺴﻨﺒ ﻲﻨﺎﻤﻭﺒﺭﻴﺘﻜﺎﺒﻭﺘﻴﻨﻴﺴﻷﺍ ،

%

22،7

ﺔـﺒﺴﻨﺒ ﻲﻜﺍﻭﻠﻜ ﺭﻴﺘﻜﺎﺒﻭﺭﻴﺘﻨﻭﻷﺍ

%

11،3

(

لﺜﻤﺘ ،

ﻡﺍﺭﻐﻟﺍ ﺔﻴﺒﺎﺠﻴﻹﺍ ﺕﺍﺭﻭﻜﻤﻟﺍ

30,5%

ﻌﻟﺍ ﺎﻬﺴﺃﺭ ﻰﻠﻋﻭ ﻡﻴﺜﺍﺭﺠﻟﺍ ﻉﻭﻤﺠﻤ ﻥﻤ

ﺔﻴﺴﺎﺴﺤ ﺕﺍﺫ ﺔﻴﻨﻬﻟﺍ ﺔﻴﺩﻭﻘﻨ

ﻥﻴﻠﺴﺘﻤﻠﻟ

)

ﺱﻤﺎﺴ

(

لﻜﺸﺘ ﻲﺘﻟﺍﻭ

24,7%

ﺱﻤﺎﺴ ﺙﻴﺤﺒ

/

ﻡﻏﺎﺴ

=

0،33

)

ﺔﻤﻭﺎﻘﻤ ﺔﻴﺒﻫﺫﻟﺍ ﺔﻴﺩﻭﻘﻨﻌﻟﺍ ﻡﻏﺎﺴ

ﻥﻴﻠﺴﺘﻤﻠﻟ

(

،

ﺔﺒﺴﻨﺒ ﺝﻭﺩﺯﻤﻟﺍ ﺝﻼﻌﻟﺍ لﺎﻤﻌﺘﺴﺍ ﻰﻠﻋ ﺱﺎﺴﻷﺎﺒ ﺔﻴﻭﻴﺤﻟﺍ ﺕﺍﺩﺎﻀﻤﻟﺎﺒ ﺝﻼﻌﻟﺍ ﺩﻤﺘﻌﻴ

%

57،8

لﺒﺎﻘﻤ

%

38،5

ﻴﻜﺭﺘﻟﺍ ﻊﻤ ﻲﺜﻼﺜﻟﺍ ﺝﻼﻌﻟﺍ لﺎﻤﻌﺘﺴﺍ ﺕﻨﻤﻀﺘ ﺔﻟﺎﺤ

ﻡﻴﻨﻴﺒﻤﻹﺍ ﻰﻠﻋ ﺎﻨﺘﻋﻭﻤﺠﻤ ﻲﻓ ﺱﺎﺴﻷﺎﺒ ﺯ

ﺔﺒﺴﻨﺒ ﺔﻴﻭﻴﺤﻟﺍ ﺕﺍﺩﺎﻀﻤﻟﺎﺒ ﺞﻬﻨﻤﻤ ﺝﻼﻋ ﺭﺎﻁﺇ ﻲﻓ ﻥﻴﺴﺎﻜﻴﻤﻷﺍﻭ

%

49

ﺔﺒﺴﻨﺒ ﻲﻟﺎﻤﺘﺤﺍ ﺝﻼﻋ لﺒﺎﻘﻤ

%

51

،

ﺏ ﺕﺎﻴﻓﻭﻟﺍ ﺔﺒﺴﻨ ﺭﺩﻘﺘ

%

51،4

لﺒﺎﻘﻤ ﺎﻨﺘﻋﻭﻤﺠﻤ ﻲﻓ

%

48،6

،ﺔﻴﺤﺼﻟﺍ ﺎﻬﺘﻴﻌﻀﻭ ﺕﻨﺴﺤﺘ ﺔﻟﺎﺤ

ﺔﻤﺩﻘﻤﻟﺍ ﺔﻴﺎﻨﻌﻟﺎﺒ ،ﺽﻴﺭﻤﻟﺍ ﺹﺌﺎﺼﺨﺒ ﺽﺭﻤﻟﺍ ﺍﺫﻫ ﺭﻴﺼﻤ ﻕﻠﻌﺘﻴ

ﺔﻴﻭﻴﺤﻟﺍ ﺕﺍﺩﺎﻀﻤﻟﺍ ﺓﺩﻤﻭ ﺔﻴﻋﻭﻨﺒﻭ

.

ﻁﻭﺭﺸ ﺓﺎﻋﺍﺭﻤ ﻰﻠﻋ ﺱﺎﺴﻷﺎﺒ ﺓﺯﻜﺘﺭﻤﻟﺍ ﺔﻴﺌﺎﻗﻭﻟﺍ ﺭﻴﺒﺍﺩﺘﻟﺍ ﻥﻤ ﺔﻋﻭﻤﺠﻤ ﺽﺭﻌﻨ ﺔﺴﺍﺭﺩﻟﺍ ﻩﺫﻫ ﺔﻴﺎﻬﻨ ﻲﻓ

ﺏﻴﻟﺎﺴﻷﺍ ﻩﺫﻬﻟ ﺔﺒﺴﻨﻟﺎﺒ ﺞﻟﺎﻌﻤﻟﺍ ﻡﻗﺎﻁﻠﻟ ﺭﻤﺘﺴﻤﻟﺍ ﻥﻴﻭﻜﺘﻟﺍﻭ ﺭﻴﻬﻁﺘﻟﺍ

.

[1] Fagon J, Chastre J, Vuagnat A, Trouillet J, Novara A, Gibert C.

Nosocomial pneumonia and mortality among patients in intensive care units. JAMA 1996;275:866–9.

[2] Bercault N, Boulain T.

Mortality rate attributable to ventilator associated nosocomial pneumonia in an adult intensive care unit: a prospective case control study.

Crit Care Med 2001;29:2303–9.

[3] Alp E, Guven M, Yildiz O, Aygen B, Voss A.

Incidence, risk factors and mortality of nosocomial pneumonia in Intensive Care Units: a prospective study.

Ann Clin Microbiol Antimicrob 2004;3:17 [4] Chastre J, Fagon JY.

Ventilator-associated pneumonia.

Am J Respir Crit Care Med 2002;165:867-903. [5] Richards MJ, Edwards JR, Culver DH, Gaynes RP.

Nososcomial infections in medical intensive care units in the United States. National Nosocomial Infections Surveillance System.

Crit Care Med 1999;27:887-92

[6] Cook D, De Jonghe B, Brochard L, Brun-Buisson C.

Influence of airway management on ventilator-associated pneumonia: evidence from randomized trials.

JAMA 1998;279:781-7.

[7] Guidelines for the management of adults with hospital-acquired. Ventilator-associated, and healthcare-associated pneumonia. Am J Respir Crit Care Med 2005; 171:388-416.

[8] Rouby J.J, Laurent P, Gosnach M, Cambau E, Lamas G, Zouaoui A.

Risk factors and clinical relevance of nosocomial maxillary sinusitis in the critically ill. Am J Respir Crit Care Med 1994;150:776-783.

[9] Ewig S, Torres A, El-Ebiary M, Fabregas N, Hernandez C, Gonzalez J

Bacterial colonization patterns in mechancally ventilated patients with traumatic and medical head injury. Incidence, risk factors, and association with ventilator-associated pneumonia. Am. J. Respir.Crit. Care. Med 1999;159:188-198

[10] Niederman MS.

The pathogenesis of airway colonization: lessons learned from the study of bacterial adherence. Eur Respir J 1994;7:1737-40.

[11] Ferrer R, Artigas A.

Clinical review: non-antibiotic strategies for preventing ventilator-associated pneumonia. Crit Care 2002;6:45-51.

[12] Collard HR, Saint S, Matthay MA.

Prevention of ventilator-associated pneumonia: an evidence-based systematic review. Ann Intern Med 2003;138:494-501.

[13] Fourrier F, Cau-Pottier E, Boutigny H, Roussel-Delvallez M, Jourdain M, Chopin C. Effects of dental plaque antiseptic decontamination on bacterial colonization and nosocomial infections in critically ill patients.

Intensive Care Med 2000;26:1239-47.

[14] Khoy-Ear L, Roux D, Gaudry S, Bex J, Dreyfuss D, Denamur E, Ricard J.-D

Impact du traitement antifongique de la colonisation des voies aériennes à candida albicans sur le développement d’une pneumopathie à Pseudomonas aeruginosa chez le rat

2009;37:1062–1067

[15] Azoulay E, Timsit JF, Tafflet M, de Lassence A, Darmon M, Zahar JR.

Candida colonization of the respiratory tract and subsequent Pseudomonas ventilator-associated pneumonia.

Chest 2006;129(1):110-7.

[16] Nseir S, Jozefowicz E, Cavestri B, Sendid B, Di Pompeo C, Dewavrin F.

Impact of antifungal treatment on Candida- Pseudomonas interaction : a preliminary retrospective casecontrol study.

Intensive Care Med 2007;33(1):137-42. [17] Stamm AM.

Ventilator-associated pneumonia and frequency of circuit changes. Am J Infect Control 1998;26:71-3.

[18] Pingleton SK, Hinthorn DR, Liu C.

Enteral nutrition in patients receiving mechanical ventilation. Multiple sources of tracheal colonization include the stomach.

[19] Ibanez J, Penafiel A, Marse P, Jorda R, Raurich JM, Mata F.

Incidence of gastroesophageal reflux and aspiration in mechanically ventilated patients using small-bore nasogastric tubes.

JPEN J Parenter Enteral Nutr 2000;24:103-6. [20] Bonten MJ, Gaillard CA.

Ventilator-associated pneumonia: do the bacteria come from the stomach? Neth J Med 1995;46:1-3.

[21] Warner DS.

Ventilator- associated pneumonia or endotracheal tube- associated pneumonia? Anesthesiology 2009;110:673-80.

[22] Nelson S, Mason C.M, Kolls J and Summer W.R. Pathophysiologie of pneumonia.

Clin Chest Med 1995;16:1-12. [23] Danin P.-E.

Structure et microbiologie du biofilm des sondes d’intubation chez le patient ventilé en réanimation.

Revue des Maladies Respiratoires 2009;26:103

[24] Adir CG, Gorman SP, Feron BM,Byers LM, Jones DS, Goldsmith CE, Moore JE, Kerr JR, Curran MD, Hogg G, Webb CH, McCarthy GJ, Milligan KR.

Implications of endotracheal tube bio-film for ventilator-associated pneumonia. Intensive Care Med 1999;25:1072-6.

[25] Dodek P.

Evidence-Based Clinical Practice Guideline for the Prevention of Ventilator-Associated Pneumonia.

Ann Intern Med 2004;14:305-13.

[26] Boulain T and Association des Réanimateurs du Centre-Ouest.

Unplanned extubations in the adult intensive care unit: a prospective multicenter study, Am J Respir Crit Care.Med 1998;157:1131–1137

[27] Rello J, Ollendorf DA, Oster G, Vera-Llonch M, Bellm L, Redman R, Kollef MH Epidemiology and outcomes of ventilator-associated pneumonia in a large us database.

[28] Sottile F.D, Marrie T.J, Prough D.S, Hobgood C.D, Gower D.J, Webb L.X.

Nosocomial pulmonary infection: possible etiologic significance of bacterial adhesion to endotracheal tubes.

Crit Care Med 1986;14:265-270. [29] Mahul P, Auboyer C, Jospe R.

Prevention of nosocomial pneumonia in intubated patients: respective role of mechanical subglottic secretions drainage and stress ulcer prophylaxis.

Intensive Care Med 1992;18: 20-5. [30] Goalson J.J.

The pathology of noscomial pneumonia. Clin Chest Med 1995;16:13-28.

[31] Guartite A, Idali B, Bouderka MA, Harti A, Louardi H and Benaguida M. Les pneumopathies nosocomiales chez le malade ventilé.

Réanimation 1995;14:37-40 [32] Niederman M.S.

Nosocomial pneumonia in the elderly patient : Chronic care facility and hospital considerations. Clin Chest Med 1993;14:479-490.

[33]Dennensen PJ, Van der Van AJ, Kessels AG, Ramsay G, Bonten MJ.

Resolution of infectious parameters after antimicrobial therapy in patients with ventilator- associated pneumonia.

Am J Respir Crit Care Med 2001;163:1371–5. [34] Donati S.Y, Demory D, Papazian L.

Pneumopathies nosocomiales acquises sous ventilation mécanique Conférences d’actualisation 2003:693-704

[35] Rammaert B, Ader F and Nseir S.

Pneumonies acquises sous ventilation mécanique invasive et bronchopneumopathie chronique obstructive.

Revue des Maladies Respiratoires 2007;24:1285-1298

[36] Jung B, Sebbane M, Chanques G, Courouble P, Cisse M, Perrigault P.-F, Jean-Pierre H, Eledjam J.-J, Jaber S,

Pneumonies acquises sous ventilation mécanique: suivez les recommandations! Annales françaises d'anesthésie et de réanimation2007;26(10) :844-849

[37] Niedermann M.S and Fein A.M.

Community acquired Pneumonia in the ederly. In: M.S. Niederman, Editor, Respiratory Infections in the ederly.

Raven Press, New York 1991:45–72

[38] El Solh AA, Al-Nabhan M, Bhora M, Dhillon R, Krauza M.

Morbid obesity is not associated with increased incidence of ventilator associated pneumonia. Proc Am Thorac Soc 2005;2:425

[39] Ibrahim EH, Tracy L, Hill C.

The occurrence of ventilator-associated pneumonia in a community hospital: risk factors and clinical outcomes.

Chest 2001;120:555-61.

[40] Cook DJ, WALTER SD, Cook RJ, Griffith LE, Guyatt GH, Leasa D, JAESCHKE rz, Brun-Buisson C. Incidence o fand risk factor for ventilator-associated pneumonia in critically ill patients.

Ann intern Med 1998;129:433-40. [41] Joshi N, Localio A, Hamory B.

A predictive risk index for nosocomial pneumonia in the intensive care unit. Am J Med 1992;93:135–42

[42] Aissaoui Y, Azendour H, Balkhi H, Haimeur C, Kamili Drissi N and Atmani M. Délai de la trachéotomie et devenir des patients sous ventilation mécanique Annales Françaises d’Anesthésie et de Réanimation 2007;26(6) :496-501 [43] Antonelli M, Conti G, Rocco M.

A comparison of non-invasive positive pressure ventilation and conventional mechanical ventilation in patients with acute lung injury.

N Engl J Med 1998;339:429–35.

[44] Girault C, Lamia B, Beduneau G and Auriant I.

La ventilation non-invasive au decours de l'intubation Réanimation. March 2005;14(2):94-103

[45] Girou E, Schortgen F, Delclaux C.

Association of non-invasive ventilation with nosocomial infections and survival in critically ill patients.

[46] Girou E, Brun-Buisson C, TaillE S, Lemaire F, Brochard L.

Secular trends in nosocomial infections and mortality associated with non-invasive ventilation in patients with exacerbation of COPD and pulmonary edema.

JAMA 2003;290:2985-91.

[47] Torres A, Serra-Batlles J, Ros E.

Pulmonary aspiration of gastric contents in patients receiving mechanical ventilation: the effect of body position.

Ann Intern Med 1992;116:540-3. [48] Choi SC, Nelson LD.

Kinetic therapy in critically ill patients: combined results based on meta-analysis. J Crit Care 1992;7:57-62.

[49] Ntoumenopoulos G, Presneill JJ, McElholum M.

Chest physiotherapy for the prevention of ventilator-associated pneumonia. Intensive Care Med 2002;28:850-6.

[50] Kreymann KG, Berger MM, Deutz NE,Hiesmayr M, Jolliet P, Kazandjiev G. Guide lineson enteral nutrition:Intensive care.

Clin Nutr 2006;25(2):210-23. [51] Thuong M,Leteurtre S.

Experts recommendation softhe. Société de réanimation de languefrançaise. Enteral nutrition in critical care.

Reanimation 2003;12:350-4.

[52] Reignier J, Vinatier I, Martin-Le fèvre L, Clementi E, Fiancette M Nutrition entérale et ventilation mécanique en décubitus ventral REAURG 2010;2875 :6

[53] Roquillya A, Lepelletierb D, Loutrela O, Demeurea D, Champina P, Mahea P, Dumonta R, Nauxb E, Lejusa C, Asehnoune K.

La nutrition entérale précoce protège les traumatisés crâniens graves des pneumopathies précoces.

Annales Françaises d’Anesthésie et de Réanimation 2009;28:236–239 [54] Ibrahim E, Mehringer L, Prentice D, Sherman G, Schaiff R, Fraser V.

Early vs late enteral feeding of mechanically ventilated patients: results of a clinical trial. J Parenter Enteral Nutr 2002;26:174–81

[55] Rello J, Diaz E, Rodriguez A.

Advances in the management of pneumonia in the intensive care unit: review of current thinking.

Clin Microbiol Infect 2005;11: 30-8.

[56] Dezfulian C, Sohjania K, Collard HR, Kim HM, MAtthay MA, Saint S.

Subglottic secretion drainage for preventing ventilator-associated pneumonia : a meta-analysis. Am J Med 2005;118:11-18

[57] Drakulovic B, Torres A, Bauer T, Nicolas J, Nogue S, Ferrer M.

Supine body position as a risk factor for nosocomial pneumonia in mechanically ventilated patients: a randomised trial.

Lancet 1999;354:1851–8.

[58] Hess DR, Kallstrom TJ, Mottram CD.

Care of the ventilator circuit and its relation to ventilator-associated pneumonia. Respir Care 2003;48:869-79.

[59] Kollef MH.

The prevention of ventilator-associated pneumonia. N Engl J Med 1999;340:627-34.

[60] Ricard JD, Paluch B, Dreyfuss D.

Efficiency and safety of mechanical ventilation with a heat and moisture exchanger changed only once a week.

Am J Respir Crit Care Med 2001;161:104-9.

[61] Liberati A, D’Amico R, Pifferi S, Torri V, Brazzi L.

Antibiotic prophylaxis to reduce respiratory tract infections and mortality in adults receiving intensive care.

Cochrane Database Syst Rev. In; 2004;1:

[62] Gastinne H, Wolff M, Delatour F, Faurisson F, Chevret S. A controlled

trial in intensive care units of selective decontamination of the digestive tract with non- absorbable antibiotics.

N Engl J Med 1992;326:594–9.

[63] Gastinne H, Wolff M, Delatour F, Faurisson F, Chevret S.

A controlled trial in intensive care units of selective decontamination of the digestive tract with nonabsorbable antibiotics. The French Study Group on Selective Decontamination of the Digestive Tract.

[64] Sanchez Garcia M, Cambronero Galache JA, Lopez Diaz J, Cerda Cerda E, Rubio Blasco J, Gomez Aguinaga MA.

Effectiveness and cost of selective decontamination of the digestive tract in critically ill intubated patients. A randomized, double-blind, placebo-controlled, multicenter trial.

Am J Respir Crit Care Med 1998;158:908–16.

[65] Silvestri L, van Saene HK, Milanese M, Fontana F, Gregori D, Oblach L.

Prevention of MRSA pneumonia by oral vancomycin decontamination: a randomised trial. Eur Respir J 2004;23:921–6.

[66] Krueger WA, Lenhart FP, Neeser G, Ruckdeschel G, Schreckhase H, Eissner HJ. Influence of combined intravenous and topical antibiotic prophylaxis on the incidence of infections, organ dysfunctions, and mortality in critically ill surgical patients: a prospective, stratified, randomized, doubleblind, placebo-controlled clinical trial.

Am J Respir Crit Care Med 2002;166:1029–37.

[67] Weigel LM, Clewell DB, Gill SR, Clark NC, McDougal LK, Flannagan SE.

Genetic analysis of a high-level vancomycin-resistant isolate of Staphylococcus aureus. Science 2003;302:1569–71.

[68] Bergmans DC, Bonten MJ, Gaillard CA, Paling JC, van der Geest S, van Tiel FH. Prevention of ventilator associated pneumonia by oral decontamination: a prospective, randomized, double- blind, placebo-controlled study.

Am J Respir Crit Care Med2001;164:382–8.

[69] Hafidia H, Gindrea S, Quintarda H, Orbana J.-C, Levrautb J, Ichaia C.

Antibioprophylaxie des pneumopathies acquises sous ventilation mécanique chez les cérébro-lésés.

Annales Françaises d’Anesthésie et de Réanimation 2009;28:236–239 [70] Tryba M.

Sucralfate versus antacids or H2-antagonists for stress ulcer prophylaxis: a meta-analysis on efficacy and pneumoniarate.

Crit Care Med 1991;19:942-949.

[71] Prod’hom G, Leuenberger P, Koerfer J, Blum A, Chiolero R, Schaller M.D.

Nosocomial pneumonia in mechanically ventilated patients receiving antacid, ranitidine, or sucralfate as prophylaxis for stress ulcer.

A randomized controlled trial. Ann Intern Med 1994;120:653-662.

[72] Navad F, Steingrub J.

Stress ulcer: is routine prophylaxis necessary? Am J Gastroenterol 1995;90:708–12.

[73] American Thoracic Society .

Hospital-acquired pneumonia in adults: diagnosis, assessment of severity,initial antimicrobial therapy, and preventive strategies. A consensus statement, November 1995.

Am J Respir Crit Care Med 1996;153:1711–25. [74] Torres A, Ewig S.

Diagnosing ventilator-associated pneumonia. N Engl J Med 2004;350:433–5.

[75] Michaud S, Suzuki S and Harbarth S.

Effect of design-related bias in studies of diagnostic tests for ventilator-associated pneumonia, Am. J. Respir. Crit. Care Med. 2002;166:1320–1325

[76] Pugin J, Auckenthaler R, Mili N, Janssens J.P, Lew P.D and Suter P.M.

Diagnosis of ventilator-associated pneumonia by bacteriologic analysis of bronchoscopic and non-bronchoscopic 'blind' bronchoalveolar lavage fluid,

Am. Rev. Respir. Dis. 1991;143:1121–1129.

[77] Singh N, Rogers P, Atwood CW, Wagener M.M and Yu V.L

Short-course empiric antibiotic therapy for patients with pulmonary infiltrates in the intensive care unit: a proposed solution for indiscriminate antibiotic prescription,

Am.Rev.Respir.Dis. 1991;143:1121-1129

[78] Luna C.M, Blanzaco D, Niederman M.S, Matarucco W, Baredes N.C and Desmeru P.

Resolution of ventilator-associated pneumonia: Prospective evaluation of the clinical pulmonary infection score as an early clinical predictor of outcome.

Crit.Care Med. 2003 ;31:676- 682 [79] Wunderink R.G.

Mortality and the diagnosis of ventilator-associated pneumonia: a new direction, Am. J. Respir. Crit. Care Med.1998;157:349–350.

[80] Flanagan P.G, Findlay G.P, Magee J.T, lonescu A, Barnes R.A and Smithies M.

The diagnosis of ventilator-associated pneumonia using non-bronchoscopic, non-directed lung lavages.

[81] Fabregas N, Ewig S, Torres A, El-Ebiary M and Rodriguez J, de la bellacasa JP.

Clinical diagnosis of ventilator associated pneumonia revisited: comparative validation using immediate post-mortem lung biopsies,

Thorax1999;54:867-873 [82] Donati S.Y, Papazian L.

Pneumopathies nosocomiales acquises sous ventilation mécanique. Anesthésie-Réanimation 2008;36:984-16

[83] Meduri G.U, Beals D.H, Maijub A.G and Baselski V.

Protected bronchoalveolar lavage. A new bronchoscopic technique to retrieve uncontaminated distal airway secretions.

Am Rev Respir Dis1991;143:855–864. [84] Fagon JY, Chastre J, Wolff M.

Invasive and noninvasive strategies for management of suspected ventilator-associated pneumonia. A randomized.

Ann Intern Med 2000;132:621-30

[85] Pham L, Brun-Buisson C, Legrand P, Rauss A, Verra F, Brochard L.

Diagnosis of nosocomial bronchopneumonia in mechanically ventilated patients. Comparison of a plugged telescoping catheter with the protected specimen brush.

Am Rev Respir Dis 1991;143:1055–61.

[86] Chollet-Martin S, Jourdain B, Gibert C, Elbim C, Chastre J and Gougerot-Pocidalo M.A. Interactions between neutrophils and cytokines in blood and alveolar spaces during ARDS. Am J Respir Crit Care Med 1996;154:594–601

[87] Fangio P, Rouquette-Vincenti I, Rousseau J.M, Soullié B and Brinquin L.

Diagnostic non invasif des pneumopathies nosocomiales acquises sous ventilation mécanique:comparaison entre le prélèvement distal protégé et l’aspiration endotrachéale, Annales Françaises d’Anesthésie et de Réanimation 2002;21:184-192

[88] de Jaeger A, Litalien C, Lacroix J, Guertin MC, Infante-Rivard C.

Protected specimen brush or bronchoalveolar lavage to diagnose bacterial nosocomial pneumonia in ventilated adults: a meta-analysis.

Crit Care Med 1999;27:2548–60. [89] Baughman RP.

Protected-specimen brush technique in the diagnosis of ventilator-associated pneumonia. Chest 2000;117:203–206.

[90] Wood A, Davit A, Ciraulo D, Arp N, Richart C, Maxwell R.

Prospective assessment of diagnostic efficacy of blind protective bronchialbrushings compared to bronchoscope-assisted lavage, bronchoscope-directed brushings, and blind endotracheal aspirates in ventilator-associated pneumonia.

J Trauma 2003;55:825–34.

[91] Elatrous S, Boukef R, Ouanes Besbes L, Marghli S, Nooman S, Nouira S.

Diagnosis of ventilator-associated pneumonia: agreement between quantitative cultures of endotracheal aspiration and plugged telescoping catheter.

Intensive Care Med 2004;30:853–8.

[92] Cavallo J.D, Leblanc F, Fabre R, Fourticq-Esqueoute A and GERPB

Surveillance de la sensibilité de Pseudomonas aeruginosae aux antibiotiques en France et distribution des mécanismes de résistance aux bétalactamines,

Pathologie Biologie ;2001;49:534-539 [93] Francioli P, Chastre J, Langer M.

Ventilator-associated pneumonia-Understanding epidemiology and pathgenesis to guide prevention and empiric therapy.

Clin Microbiol Infect 1997;3:61-76 [94] Campbell GD.

Blinded invasive procedures in ventilator-associated pneumonia. Chest 2000;117:207-211.

[95] Cook D, Mandell L.

Endotracheal aspiration in the diagnosis of ventilator-associated pneumonia. Chest 2000; 117:195-197

[96] Torres A, El-Biary M.

Bronchoscopic BAL in the diagnosis of ventilor-associated pneumonia. Chest 2000;117: 198-202.

[97] Marquette C., Copin M., Wallet F., Neviere R., Saulnier F., Mathieu D.

Diagnostic tests for pneumonia in ventilated patients:prospective avaluation of diagnostic accuracy using histology as a diagnostic gold standard.

Am. Rav. Respir. Dis 1995;151:1878-8

[98] Torres A., El-Ebiary M., Padro L., Gonzalez J., Puig de la Bellacasa J., Ramirez J.

Validation of different techniques for the diagnosis of ventilator-associated pneumonia. Comparison with immediate postmortem pulmonary biopsy.

[99] Chastre J., Fagon J.-Y., Bornet-Lecso M., Calvat S., Dombret M.-C., Al Khani R. Evaluation of bronchoscopic techniques for the diagnosis of nosocomial pneumonia. Am. J. Respir. Crit. Care Med. 1995;152: 231-240

[100] Kirtland S.H., Corley D.E., Winterbauer R.H., Springmeyer S.C., Casey K.R., Hampson N.B., Dreis D.F.

The diagnosis of ventilator-associated pneumonia. Acomparison of histologic, microbiologic, and clinical criteria.

Chest, 1997;112:444-457

[101] Papazian L.,Thomas P.,Garbe L. et coll

Bronchoscopic or blind sampling techniques fort he diagnosis of ventilator-associated pneumonia.

Am. J. Resp.Crit.Care Med 1995;152:1982-91 [102] Fagon J.Y.

Epidémiologie et antibiothérapie des pneumopathies nosocomiales.

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